Trials / Not Yet Recruiting
Not Yet RecruitingNCT07234292
Evaluation of Patient Satisfaction With Blephaderm as a Complementary Care in Post-eyelid Surgery.
Evaluation of Patient Satisfaction With a New Preservative-free Eyelid Cream as a Complementary Care in Post-eyelid Surgery: The ADMIRE Study
- Status
- Not Yet Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 30 (estimated)
- Sponsor
- Laboratoires Thea · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this non-interventional, open and monocentric study is to evaluate the satisfaction of 30 patients, after 3 months with Blephaderm eyelid cream, as a complementary care in post-eyelid surgery (Blepharopasty or ptosis). The participant will be asked to use Blephaderm twice a day. The patient satisfaction will be evaluated using a VAS scale.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Cosmetic: Blephaderm | Preservative free eyelid cream: Aqua (water), oleyl erucate, trehalose, sodium acrylates copolymer, lecithin, Ophiopogon japonicus root extract, hydrolyzed hyaluronic acid, maltodextrin, tocopherol, sodium hydroxide, phytic acid, Glycine soja (soybean) oil, Helianthus annuus seed oil. |
Timeline
- Start date
- 2025-11-15
- Primary completion
- 2026-05-15
- Completion
- 2026-05-15
- First posted
- 2025-11-18
- Last updated
- 2025-11-18
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT07234292. Inclusion in this directory is not an endorsement.